Ulnar-mammary syndrome.

Author:

Schinzel A

Publisher

BMJ

Subject

Genetics(clinical),Genetics

Reference10 articles.

1. Mendelian inheritance in man. Catalogs of autosomal dominant, autosomal recessive and X-linked pheno2 types;McKusick, V.A.,1975

2. Mendelian inheritance in man. Catalogs of autosomal dominant, autosomal recessive and X-linked phenotypes;McKusick, V.A.,1986

3. Studies of malformation syndromes in man. XXXXII. A pleiotropic dominant mutation affecting skeletal, sexual and apocrine-mammary development;Pallister, P.D.; Herrmann, J.; Opitz, J.M.;Birth Defects,1976

4. Studies of malformation syndromes in man. XXXXIIB. Mother and son affected with the ulnar-mammary syndrome type Pallister;Gonzales, C.H.; Herrmann, J.; Optiz, J.M.;Eur J Pediatr,1976

5. Mendelian inheritance in man. Catalogs of autosomal dominant, autosomal recessive and X-linked phenotypes;McKusick, V.A.,1978

Cited by 45 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Surgical Treatment of Ulnar Cleft Hand with All Fingers – A Report of Two Patients;The Journal of Hand Surgery (Asian-Pacific Volume);2022-02

2. The cloning era and the cloning of Brachury and other T/t complex genes;Twentieth Century Mouse Genetics;2022

3. Central Deficiency (Cleft Hand);Congenital Anomalies of the Upper Extremity;2021

4. A de novo TBX3 mutation presenting as dorsalization of the little fingers: A forme fruste phenotype of ulnar-mammary syndrome;European Journal of Medical Genetics;2020-01

5. Ulnar-Mammary Syndrome;Atlas of Genetic Diagnosis and Counseling;2017

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3